Variant #0000980746 (NC_000014.8:g.102894581_102894582del, NC_000014.8(NM_014844.3):c.952-6_952-5del (TECPR2))

Chromosome 14
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.102894581_102894582del
DNA change (hg38) -
Published as TECPR2(NM_014844.5):c.952-6_952-5delTG
ISCN -
DB-ID CINP_000015
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TECPR2 NM_014844.3 -?/. - c.952-6_952-5del r.spl? p.?
CINP NM_032630.2 -?/. - c.-65394_-65393del r.(?) p.(=)


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